Department of Radiation Oncology, UPMC Hillman Cancer Center, Pittsburgh, PA.
Radiation Oncology, AdventHealth Cancer Institute, Orlando, FL.
Brachytherapy. 2023 Nov-Dec;22(6):808-821. doi: 10.1016/j.brachy.2023.07.005. Epub 2023 Aug 28.
This study evaluates long-term patient-reported bowel quality of life (QOL), rectal bleeding, and bleeding bother in patients with prostate cancer treated with external beam radiation therapy (EBRT) and Cesium-131 LDR brachytherapy (LDR-BT) boost with and without hydrogel rectal spacer.
This is a retrospective analysis of prostate cancer patients treated between 2007 and 2022 with 45 Gy EBRT followed by 85 Gy Cs-131 LDR-BT boost with or without hydrogel rectal spacer. Expanded Prostate Cancer Index Composite (EPIC) QOL questionnaires pre-treatment and at each follow-up were collected. Patient-reported rectal bleeding occurring more than "rarely" and bother from rectal bleeding occurring more than a "very small problem" were deemed clinically significant. Fisher's exact test was used to test the association of rectal spacer use and the incidence of clinically significant rectal bleeding and bleeding bother. Paired samples t-test was used to analyze mean bowel scores at each time point.
Three hundred and forty-one patients were included in the analysis. The rectal spacer was used in 108 patients. Overall median follow-up was 48 months (IQR, 24-72), with a median follow-up of 24 months (IQR, 12-37.5) for the hydrogel group and 60 months (IQR, 36-84) for the non-hydrogel group. EPIC questionnaire response rates at median follow-up were 33% and 37% for the hydrogel and non-hydrogel groups, respectively. A clinically significant decrease in mean bowel domain scores was seen in the bowel bother domain at 6 and 12 months for patients who did not receive a rectal spacer. At the last follow-up of 60 months, the prevalence of clinically significant rectal bleeding and bleeding bother were 2.2% and 2.2%, respectively. The cumulative incidence of clinically significant long-term rectal bleeding was 2.8% and 18.9% in the hydrogel group and non-hydrogel group, respectively (Fisher's exact test, p < 0.0001). The cumulative incidence of clinically significant long-term bowel bother was 4.6% and 19.7% in the hydrogel group and non-hydrogel group, respectively (Fisher's exact test, p < 0.001).
Use of hydrogel rectal spacer with EBRT and Cs-131 LDR-BT boost was significantly associated with a lower incidence of patient-reported rectal bleeding and bother from rectal bleeding, and better long-term bowel QOL. Cumulative incidence was 2.8% (hydrogel group) versus 18.9% (non-hydrogel group) and 4.6% (hydrogel group) versus 19.7% (non-hydrogel group) for clinically significant long-term rectal bleeding and long-term bleeding bother, respectively.
本研究评估了接受外照射放射治疗(EBRT)和铯-131 低剂量率(LDR)近距离放射治疗(LDR-BT)加或不加水凝胶直肠间隔器的前列腺癌患者的长期患者报告的肠道生活质量(QOL)、直肠出血和出血困扰。
这是对 2007 年至 2022 年间接受 45 Gy EBRT 后接受 85 Gy Cs-131 LDR-BT 加或不加水凝胶直肠间隔器治疗的前列腺癌患者进行的回顾性分析。收集了治疗前和每次随访时的扩展前列腺癌指数综合量表(EPIC)QOL 问卷。将发生“不常”以上频率的直肠出血和发生“非常小的问题”以上程度的出血困扰视为具有临床意义。使用 Fisher 确切检验来检验直肠间隔器使用与临床显著直肠出血和出血困扰的发生率之间的关联。使用配对样本 t 检验分析每个时间点的平均肠道评分。
共纳入 341 例患者进行分析。108 例患者使用了直肠间隔器。总体中位随访时间为 48 个月(IQR,24-72),水凝胶组中位随访时间为 24 个月(IQR,12-37.5),非水凝胶组为 60 个月(IQR,36-84)。在中位随访时,水凝胶组和非水凝胶组的 EPIC 问卷应答率分别为 33%和 37%。未接受直肠间隔器的患者在 6 个月和 12 个月时,在肠道困扰领域的平均肠道评分出现了具有临床意义的下降。在最后一次 60 个月的随访中,临床显著直肠出血和出血困扰的发生率分别为 2.2%和 2.2%。水凝胶组和非水凝胶组的临床显著长期直肠出血累积发生率分别为 2.8%和 18.9%(Fisher 确切检验,p<0.0001)。水凝胶组和非水凝胶组的临床显著长期肠道困扰的累积发生率分别为 4.6%和 19.7%(Fisher 确切检验,p<0.001)。
在 EBRT 和 Cs-131 LDR-BT 加量治疗中使用水凝胶直肠间隔器与较低的患者报告直肠出血发生率和直肠出血困扰率以及更好的长期肠道 QOL 显著相关。临床显著长期直肠出血和长期出血困扰的累积发生率分别为 2.8%(水凝胶组)与 18.9%(非水凝胶组)和 4.6%(水凝胶组)与 19.7%(非水凝胶组)。